CASCADE screening and registry of familial hypercholesterolemia in Iran: Rationale and design

BACKGROUND: Familial hypercholesterolemia (FH) is one of the most common genetic disorders, which leads to premature coronary artery disease (CAD). It has been suggested that heterozygous FH affects around 1:250 to 1:500 in the general population or even more than this, and homozygous FH affects 1:1...

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Detalles Bibliográficos
Autores principales: Vaseghi, Golnaz, Arabi, Sina, Haghjooy-Javanmard, Shaghayegh, Sabri, Mohammadreza, Sadeghi, Masoumeh, Khosravi, Alireza, Zarfeshani, Sonia, Sarrafzadegan, Nizal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Isfahan Cardiovascular Research Center, Isfahan University of Medical Sciences 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679656/
https://www.ncbi.nlm.nih.gov/pubmed/31440286
http://dx.doi.org/10.22122/arya.v15i2.1899

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679656/
https://www.ncbi.nlm.nih.gov/pubmed/31440286
http://dx.doi.org/10.22122/arya.v15i2.1899

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